Computational modeling and synthesis of pyridine variants of benzoyl-phenoxy-acetamide with high glioblastoma cytotoxicity and brain tumor penetration von Ingraham, Charles H., Stalinska, Joanna, Carson, Sean C., Colley, Susan B., Rak, Monika, Lassak, Adam, Peruzzi, Francesca, Reiss, Krzysztof, Jursic, Branko S.

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Synthesis and antifungal activity of substituted 2,4,6-pyrimidinetrione carbaldehyde hydrazones von Neumann, Donna M., Cammarata, Amy, Backes, Gregory, Palmer, Glen E., Jursic, Branko S.

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Anti-glioblastoma effects of phenolic variants of benzoylphenoxyacetamide (BPA) with high potential for blood brain barrier penetration von Stalinska, Joanna, Vittori, Cecilia, Ingraham IV, Charles H., Carson, Sean C., Plaisance-Bonstaff, Karlie, Lassak, Adam, Faia, Celeste, Colley, Susan B., Peruzzi, Francesca, Reiss, Krzysztof, Jursic, Branko S.

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Synthesis and antifungal activity of substituted salicylaldehyde hydrazones, hydrazides and sulfohydrazides von Backes, Gregory L., Neumann, Donna M., Jursic, Branko S.

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Exploring anticancer activity of structurally modified benzylphenoxyacetamide (BPA); I: Synthesis strategies and computational analyses of substituted BPA variants with high anti-g... von Stalinska, Joanna, Houser, Lisa, Rak, Monika, Colley, Susan B., Reiss, Krzysztof, Jursic, Branko S.

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Anticancer potential of aminomethylidene-diazinanes I. Synthesis of arylaminomethylidene of diazinetriones and its cytotoxic effects tested in glioblastoma cells von Pianovich, Nichole A., Dean, Mathew, Lassak, Adam, Reiss, Krzysztof, Jursic, Branko S.

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Potent antimicrobial agents against azole-resistant fungi based on pyridinohydrazide and hydrazomethylpyridine structural motifs von Backes, Gregory L., Jursic, Branko S., Neumann, Donna M.

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Synthesis of N-aryl and N-arylcarbamoylamino derivatives of 1,3-diazinane-5-carboxamide and their activity against glioblastoma LN-229 cell line von Hron, Rebecca J., Jursic, Branko S., Neumann, Donna M.

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Preparation of dibarbiturates of oxindole by condensation of isatin and barbituric acid derivatives von Jursic, Branko S, Stevens, Edwin D

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Trafficking through the late endosome significantly impacts Candida albicans tolerance of the azole antifungals von Luna-Tapia, Arturo, Kerns, Morgan E, Eberle, Karen E, Jursic, Branko S, Palmer, Glen E

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Cyclomaltooligosaccharide (cyclodextrin)-assisted enantiomeric recognition of benzo[ lmn][3,8]phenanthroline-derived amino acids von Jursic, Branko S., Patel, Paresh K.

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Preparation of 5-diaminomethylenebarbiturates by barbituric acid addition to carbodiimides von Jursic, Branko S, Douelle, Fred, Stevens, Edwin D

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Comparison of microwave-assisted and conventional preparations of cyclic imides von Upadhyay, Sunil K., Pingali, Subramanya R.K., Jursic, Branko S.

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NMR spectroscopic study of cyclodextrin inclusion complexes with A-007 prodrugs von Sagiraju, Sarada, Jursic, Branko S.

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Anticancer activity for 4,4′-Dihydroxybenzophenone-2,4-dinitrophenylhydrazone (A-007) analogues and Their abilities to interact with lymphoendothelial cell surface markers von Morgan, Lee Roy, Jursic, Branko S., Hooper, Catherine L., Neumann, Donna M., Thangaraj, Kanappan, LeBlanc, Blaise

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Microwave-assisted benzyl mono- and dibromination in diethyl carbonate as environmentally friendly alternative to radical bromination in carbon tetrachloride von PINGALI, Subramanya R. K, UPADHYAY, Sunil K, JURSIC, Branko S

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Antifungal activity of 2α,3β-functionalized steroids stereoselectively increases with the addition of oligosaccharides von Cammarata, Amy, Upadhyay, Sunil Kumar, Jursic, Branko S., Neumann, Donna M.

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Microwave-assisted synthesis of 1,3-benzodioxole derivatives from catechol and ketones or aldehydes von Pingali, Subramanya R.K., Jursic, Branko S.

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Novel and efficient synthesis and antifungal evaluation of 2,3-functionalized cholestane and androstane derivatives von Jursic, Branko S., Upadhyay, Sunil Kumar, Creech, Clinton C., Neumann, Donna M.

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Preparation of tagged glucose as a key intermediate in the synthesis of branched oligosaccharides von Upadhyay, Sunil K., Jursic, Branko S.

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